6-Methoxy-2-naphthoic Acid - ≥97% , CAS No.2471-70-7

CAS: 2471-70-7 Cat. No.: M132856 Molecular Weight: 202.21 Beilstein Registry Number: 10(4)1194 EC Number: 607-425-6
AVAILABLE TO ORDER
GRADE & PURITY ≥97%
Synonyms
6-Methoxy-naphthalene-2-carboxylic acid | 6-methoxynaphthalene-2-carboxylic acid | 6-Methoxy-2-naphthalenecarboxylic acid | 6-Methoxy-2-naphthalene carboxylic acid | SR-01000495891-1 | UNII-65IH1SV66A | 2-Naphthoic acid, 6-methoxy- | 6-Methoxy-2-naphthoic
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Status
Price
Qty
1g
M132856-1g
3

$15.90

$23.90
Save $8.00 (33.47%)
5g
M132856-5g
5

$26.90

$40.90
Save $14.00 (34.23%)
10g
M132856-10g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.

$40.90

$61.90
Save $21.00 (33.93%)
25g
M132856-25g
5

$72.90

$109.90
Save $37.00 (33.67%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature Ships Normal Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonyms
6-Methoxy-naphthalene-2-carboxylic acid | 6-methoxynaphthalene-2-carboxylic acid | 6-Methoxy-2-naphthalenecarboxylic acid | 6-Methoxy-2-naphthalene carboxylic acid | SR-01000495891-1 | UNII-65IH1SV66A | 2-Naphthoic acid, 6-methoxy- | 6-Methoxy-2-naphthoic
Specifications & Purity
≥97%
Storage
Room temperature
Shipped In
Normal
Purity
≥97%
Names and Identifiers
Pubchem Sid504758552
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504758552
Canonical SmilesCOC1=CC2=C(C=C1)C=C(C=C2)C(=O)O
IUPAC Name6-methoxynaphthalene-2-carboxylic acid
InChIKeyYZBILXXOZFORFE-UHFFFAOYSA-N
INCHI1S/C12H10O3/c1-15-11-5-4-8-6-10(12(13)14)3-2-9(8)7-11/h2-7H,1H3,(H,13,14)
Isomeric SMILES COC1=CC2=C(C=C1)C=C(C=C2)C(=O)O
WGK Germany 3
Molecular Weight 202.21
Beilstein 10(4)1194
Reaxy-Rn 2211233
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2211233&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
ClassNaphthalenes
SubclassNaphthalenecarboxylic acids and derivatives
Intermediate Tree Nodes Not available
Direct ParentNaphthalenecarboxylic acids
Alternative Parents Anisoles  Alkyl aryl ethers  Carboxylic acids  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic homopolycyclic compounds
Substituents 2-naphthalenecarboxylic acid - Phenol ether - Anisole - Alkyl aryl ether - Ether - Carboxylic acid - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Aromatic homopolycyclic compound
DescriptionThis compound belongs to the class of organic compounds known as naphthalenecarboxylic acids. These are compounds containing a naphthalene moiety, which bears a carboxylic acid group one or more positions. Naphthalene is a bicyclic compound that is made up of two fused benzene ring.
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
KDM4E Tchem Lysine-specific demethylase 4D-like (40243 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GCN5 Histone acetyltransferase GCN5 (89 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Dyrk1a Dual specificity tyrosine-phosphorylation-regulated kinase 1A (1629 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Luciferin 4-monooxygenase (66902 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NS1 Nonstructural protein 1 (33327 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mechanisms of Action
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

5 results found

Lot NumberCertificate TypeDateItem
I2222186Certificate of AnalysisApr 03, 2026 M132856
I2222187Certificate of AnalysisApr 03, 2026 M132856
I2222291Certificate of AnalysisApr 03, 2026 M132856
A1705111Certificate of AnalysisFeb 05, 2026 M132856
F2215132Certificate of AnalysisDec 12, 2025 M132856
Chemical and Physical Properties
Melt Point(°C)201-206 °C
Molecular Weight202.210 g/mol
XLogP33.300
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count3
Rotatable Bond Count2
Exact Mass202.063 Da
Monoisotopic Mass202.063 Da
Topological Polar Surface Area46.500 Ų
Heavy Atom Count15
Formal Charge0
Complexity239.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Solution Calculators
Reviews

Customer Reviews

Shall we send you a message when we have discounts available?

Remind me later

Thank you! Please check your email inbox to confirm.

Oops! Notifications are disabled.